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Kousseff, Boris G.
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1

Triploidy and trisomies in the offspring of a mother with a..:

Slavin, Thomas P. ; Kousseff, Boris G.
Prenatal Diagnosis.  25 (2005)  7 - p. 623-624 , 2005
Link: https://doi.org/10.1002/..
 
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2

Omphalocele and gastroschisis: An 18-year review study:

Hwang, Pei-Jen ; Kousseff, Boris G.
Genetics in Medicine.  6 (2004)  4 - p. 232-236 , 2004
Link: https://doi.org/10.1097/..
 
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3

Three cell line mosaicism involving structural and numerica..:

Sutcliffe, Maxine J. ; Mueller, O. Thomas ; Kousseff, Boris G....
American Journal of Medical Genetics.  102 (2001)  2 - p. 192-199 , 2001
Link: https://doi.org/10.1002/..
 
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4

Penile neurofibromas:

Kousseff, Boris G. ; Hoover, Dennis L.
American Journal of Medical Genetics.  87 (1999)  1 - p. 1-5 , 1999
Link: https://doi.org/10.1002/..
 
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5

Gestational diabetes mellitus (class A): A human teratogen?:

Kousseff, Boris G.
American Journal of Medical Genetics.  83 (1999)  5 - p. 402-408 , 1999
Link: https://doi.org/10.1002/..
 
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6

'New' manifestations of BOR syndrome:

Weber, Karen M ; Kousseff, Boris G
Clinical Genetics.  56 (1999)  4 - p. 306-312 , 1999
Link: https://doi.org/10.1034/..
 
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7

Diabetic embryopathy:

Kousseff, Boris G.
Current Opinion in Pediatrics.  11 (1999)  4 - p. 348-352 , 1999
Link: https://doi.org/10.1097/..
 
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8

Analysis of CpG C‐to‐T mutations in neurofibromatosis type :

Krkljus, Sofia ; Abernathy, Corinne R. ; Johnson, Jennifer S....
Human Mutation.  11 (1998)  5 - p. 411-411 , 1998
Link: https://doi.org/10.1002/..
 
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9

Analysis of CpG C-to-T mutations in neurofibromatosis type :

Krkljus, Sofia ; Abernathy, Corinne R. ; Johnson, Jennifer S....
Human Mutation.  11 (1998)  5 - p. 411-411 , 1998
Link: https://doi.org/10.1002/..
 
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10

NF1 mutation analysis using a combined heteroduplex/SSCP ap..:

Abernathy, Corinne R. ; Rasmussen, Sonja A. ; Stalker, Heather J....
Human Mutation.  9 (1997)  6 - p. 548-554 , 1997
Link: https://doi.org/10.1002/..
 
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11

NF1 mutation analysis using a combined heteroduplex/SSCP ap..:

Abernathy, Corinne R. ; Rasmussen, Sonja A. ; Stalker, Heather J....
Human Mutation.  9 (1997)  6 - p. 548-554 , 1997
Link: https://doi.org/10.1002/..
 
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12

Multiple Endocrine Neoplasia 2 (Men 2)/Men 2A (Sipple Syndr..:

Kousseff, Boris G.
Dermatologic Clinics.  13 (1995)  1 - p. 91-97 , 1995
Link: https://doi.org/10.1016/..
 
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13

Fragile X syndrome: Discordant levels of CGG repeat mosaici..:

Mueller, O. Thomas ; Hartsfield Jr., James K. ; Amar, Marcelo J. A...
American Journal of Medical Genetics.  60 (1995)  4 - p. 302-306 , 1995
Link: https://doi.org/10.1002/..
 
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14

Peripheral neuropathy in Ehlers-Danlos syndrome:

Galan, Enrique ; Kousseff, Boris G.
Pediatric Neurology.  12 (1995)  3 - p. 242-245 , 1995
Link: https://doi.org/10.1016/..
 
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15

Uniparental isodisomy of chromosome 14 in two cases: An abn..:

Papenhausen, Peter R. ; Mueller, O. Thomas ; Johnson, Virginia P....
American Journal of Medical Genetics.  59 (1995)  3 - p. 271-275 , 1995
Link: https://doi.org/10.1002/..
 
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